Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Fbh1 ENSRNOG00000018549

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Description

F-box DNA helicase 1 [Source:RGD Symbol;Acc:1306298]

Gene Synonyms

Fbxo18, LOC291293

Location

Primary_assembly 17: 71,659,249-71,697,432 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 3 transcripts (splice variants), 197 orthologues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000170477.1	Fbh1-203	3660	1042aa	ENSRNOP00000105146.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JLR6	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENSRNOT00000127043.1	Fbh1-202	3684	968aa	ENSRNOP00000103934.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000025228.9	Fbh1-201	3451	1013aa	ENSRNOP00000025228.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M298	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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